Perognathus longimembris pacificus isolate PPM17 chromosome 12, ASM2315922v1, whole genome shotgun sequence.
Perognathus longimembris pacificus (Pacific pocket mouse)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Castorimorpha; Heteromyidae; Perognathinae; Perognathus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM041275.1.\nAssembly name: ASM2315922v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the San Diego Zoo Wildlife\nAlliance on 2022/04/27. The original whole-genome shotgun project\nhas the accession JALGBO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: San Diego Zoo Wildlife Alliance\nAssembly Date :: 2021\nAssembly Method :: Peregrine v. JUNE-2020; HiRise v.\n JULY-2020; Juicer v. DECEMBER-2020;\n Juicebox Assembly Tools v. DECEMBER-2020\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 23.0x\nSequencing Technology :: PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Perognathus longimembris pacificus\n Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
5-hydroxyisourate hydrolase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
5-hydroxyisourate hydrolase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
5-hydroxyisourate hydrolase-like isoform X1
5-hydroxyisourate hydrolase-like isoform X2
COORDINATES: polyA evidence [ECO:0006239]
zinc finger protein 250, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein 250, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
COMM domain containing 5, transcript variant X2
COMM domain containing 5, transcript variant X1
COMM domain-containing protein 5 isoform X1
COMM domain-containing protein 5 isoform X2
zinc finger protein 7, transcript variant X3
zinc finger protein 7, transcript variant X1
zinc finger protein 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 251, transcript variant X4
zinc finger protein 251, transcript variant X2
zinc finger protein 251, transcript variant X3
zinc finger protein 251, transcript variant X1
Rho GTPase activating protein 39, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Rho GTPase activating protein 39, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Rho GTPase activating protein 39, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rho GTPase activating protein 39, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
rho GTPase-activating protein 39 isoform X1
rho GTPase-activating protein 39 isoform X2
leucine rich repeat containing 24, transcript variant X2
leucine rich repeat containing 24, transcript variant X1
leucine-rich repeat-containing protein 24
leucine rich repeat containing 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leucine rich repeat containing 14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
leucine-rich repeat-containing protein 14
RecQ like helicase 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
RecQ like helicase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RecQ like helicase 4, transcript variant X2
RecQ like helicase 4, transcript variant X3
ATP-dependent DNA helicase Q4 isoform X4
ATP-dependent DNA helicase Q4 isoform X1
ATP-dependent DNA helicase Q4 isoform X2
ATP-dependent DNA helicase Q4 isoform X3
major facilitator superfamily domain containing 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
major facilitator superfamily domain containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 3
alanine aminotransferase 1, transcript variant X1
alanine aminotransferase 1, transcript variant X2
alanine aminotransferase 1, transcript variant X6
alanine aminotransferase 1, transcript variant X7
alanine aminotransferase 1, transcript variant X4
alanine aminotransferase 1, transcript variant X8
alanine aminotransferase 1, transcript variant X5
protein phosphatase 1 regulatory subunit 16A isoform X1
alanine aminotransferase 1, transcript variant X3
protein phosphatase 1 regulatory subunit 16A isoform X3
kinesin family member C2, transcript variant X1
kinesin family member C2, transcript variant X2
cysteine and histidine-rich protein 1, transcript variant X3
cysteine and histidine-rich protein 1, transcript variant X4
cysteine and histidine-rich protein 1 isoform X4
cysteine and histidine-rich protein 1 isoform X3
cysteine and histidine-rich protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cysteine and histidine-rich protein 1, transcript variant X1
cysteine and histidine-rich protein 1 isoform X1
cysteine and histidine-rich protein 1-A isoform X2
tonsoku like, DNA repair protein, transcript variant X2
tonsoku like, DNA repair protein, transcript variant X4
tonsoku like, DNA repair protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
tonsoku like, DNA repair protein, transcript variant X3
VPS28 subunit of ESCRT-I, transcript variant X1
VPS28 subunit of ESCRT-I, transcript variant X2
vacuolar protein sorting-associated protein 28 homolog isoform X1
vacuolar protein sorting-associated protein 28 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cleavage and polyadenylation specific factor 1, transcript variant X2
cleavage and polyadenylation specific factor 1, transcript variant X1
cleavage and polyadenylation specificity factor subunit 1
aarF domain containing kinase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
aarF domain containing kinase 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized aarF domain-containing protein kinase 5 isoform X1
uncharacterized aarF domain-containing protein kinase 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 27% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 52 member 2, transcript variant X1
solute carrier family 52 member 2, transcript variant X2
solute carrier family 52, riboflavin transporter, member 2 isoform X1
solute carrier family 52, riboflavin transporter, member 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cation channel sperm-associated auxiliary subunit TMEM249
scratch family transcriptional repressor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
diacylglycerol O-acyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
diacylglycerol O-acyltransferase 1, transcript variant X1
heat shock transcription factor 1, transcript variant X3
heat shock transcription factor 1, transcript variant X1
heat shock transcription factor 1, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: magnesium transporter NIPA2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
basic helix-loop-helix transcription factor scleraxis
maestro heat like repeat family member 1, transcript variant X3
maestro heat like repeat family member 1, transcript variant X4
maestro heat like repeat family member 1, transcript variant X5
maestro heat like repeat family member 1, transcript variant X1
maestro heat like repeat family member 1, transcript variant X2
maestro heat like repeat family member 1, transcript variant X6
maestro heat-like repeat-containing protein family member 1 isoform X2
maestro heat-like repeat-containing protein family member 1 isoform X1
maestro heat-like repeat-containing protein family member 1 isoform X3
maestro heat-like repeat-containing protein family member 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
testis-specific serine/threonine-protein kinase 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
MAF1 homolog, negative regulator of RNA polymerase III, transcript variant X3
MAF1 homolog, negative regulator of RNA polymerase III, transcript variant X2
MAF1 homolog, negative regulator of RNA polymerase III, transcript variant X1
MAF1 homolog, negative regulator of RNA polymerase III, transcript variant X4
repressor of RNA polymerase III transcription MAF1 homolog isoform X1
repressor of RNA polymerase III transcription MAF1 homolog isoform X2
SHANK associated RH domain interactor, transcript variant X2
SHANK associated RH domain interactor, transcript variant X1
SHANK associated RH domain interactor, transcript variant X4
SHANK associated RH domain interactor, transcript variant X3
SHANK associated RH domain interactor, transcript variant X5
cytochrome c1, heme protein, mitochondrial
glycosylphosphatidylinositol anchor attachment 1
glycosylphosphatidylinositol anchor attachment 1 protein
5-oxoprolinase, ATP-hydrolysing, transcript variant X1
5-oxoprolinase, ATP-hydrolysing, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: sphingomyelin phosphodiesterase 5-like
spermatogenesis and centriole associated 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
glutamate ionotropic receptor NMDA type subunit associated protein 1
proline-rich protein HaeIII subfamily 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
poly(ADP-ribose) polymerase family member 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
protein mono-ADP-ribosyltransferase PARP10
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 14 bases in 14 codons; deleted 33 bases in 31 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 14 bases in 14 codons; deleted 33 bases in 31 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
poly(U) binding splicing factor 60, transcript variant X1
poly(U) binding splicing factor 60, transcript variant X3
poly(U) binding splicing factor 60, transcript variant X2
poly(U) binding splicing factor 60, transcript variant X4
poly(U)-binding-splicing factor PUF60 isoform X1
poly(U)-binding-splicing factor PUF60 isoform X3
poly(U)-binding-splicing factor PUF60 isoform X2
poly(U)-binding-splicing factor PUF60 isoform X4
poly(U) binding splicing factor 60, transcript variant X6
poly(U) binding splicing factor 60, transcript variant X5
poly(U)-binding-splicing factor PUF60 isoform X5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein scribble homolog
IQ motif and ankyrin repeat containing 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: IQ motif and ankyrin repeat domain-containing protein 1
family with sequence similarity 83 member H, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
family with sequence similarity 83 member H, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 166
zinc finger protein 623, transcript variant X3
zinc finger protein 623, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 623, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 623, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
GDP-L-fucose synthase, transcript variant X2
GDP-L-fucose synthase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
tigger transposable element-derived protein 5
eukaryotic translation elongation factor 1 delta, transcript variant X4
eukaryotic translation elongation factor 1 delta, transcript variant X5
eukaryotic translation elongation factor 1 delta, transcript variant X1
eukaryotic translation elongation factor 1 delta, transcript variant X2
eukaryotic translation elongation factor 1 delta, transcript variant X3
nicotinate phosphoribosyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
nicotinate phosphoribosyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
nicotinate phosphoribosyltransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nicotinate phosphoribosyltransferase isoform X1
nicotinate phosphoribosyltransferase isoform X2
maestro heat like repeat family member 6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: maestro heat-like repeat-containing protein family member 6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger CCCH domain-containing protein 3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC125360997
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor MafA
glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 isoform X2
glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytochrome P450 11B2, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ly-6/neurotoxin-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ly-6/neurotoxin-like protein 1, transcript variant X2
secreted LY6/PLAUR domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
secreted LY6/PLAUR domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
secreted Ly-6/uPAR domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
secreted Ly-6/uPAR-related protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
LOW QUALITY PROTEIN: secreted Ly-6/uPAR-related protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: prostate stem cell antigen
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
activity regulated cytoskeleton associated protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
activity-regulated cytoskeleton-associated protein
maestro heat-like repeat family member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 4 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 4 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: adhesion G protein-coupled receptor B1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: t-SNARE domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC125360483
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: maestro heat-like repeat family member 5
LOW QUALITY PROTEIN: protein tyrosine phosphatase type IVA 3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: G-protein coupled receptor 20
solute carrier family 45 member 4, transcript variant X1
solute carrier family 45 member 4, transcript variant X2
solute carrier family 45 member 4, transcript variant X3
DENN domain containing 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DENN domain-containing protein 3 isoform X3
DENN domain-containing protein 3 isoform X1
DENN domain-containing protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein tyrosine kinase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein tyrosine kinase 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine kinase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein tyrosine kinase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein tyrosine kinase 2, transcript variant X3
protein tyrosine kinase 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein tyrosine kinase 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein tyrosine kinase 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein tyrosine kinase 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
chromatin accessibility complex subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
chromatin accessibility complex protein 1
trafficking protein particle complex subunit 9, transcript variant X1
trafficking protein particle complex subunit 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
trafficking protein particle complex subunit 9 isoform X1
trafficking protein particle complex subunit 9 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
potassium two pore domain channel subfamily K member 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 135 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
KH RNA binding domain containing, signal transduction associated 3, transcript variant X2
KH RNA binding domain containing, signal transduction associated 3, transcript variant X1
KH domain-containing, RNA-binding, signal transduction-associated protein 3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
zinc finger and AT-hook domain containing
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 1
N-myc downstream regulated 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
N-myc downstream regulated 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
N-myc downstream regulated 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cellular communication network factor 4, transcript variant X1
cellular communication network factor 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
PHD finger protein 20 like 1, transcript variant X2
PHD finger protein 20 like 1, transcript variant X8
PHD finger protein 20 like 1, transcript variant X12
PHD finger protein 20 like 1, transcript variant X11
PHD finger protein 20 like 1, transcript variant X7
PHD finger protein 20 like 1, transcript variant X6
PHD finger protein 20 like 1, transcript variant X5
PHD finger protein 20 like 1, transcript variant X3
PHD finger protein 20 like 1, transcript variant X10
PHD finger protein 20 like 1, transcript variant X4
PHD finger protein 20 like 1, transcript variant X1
PHD finger protein 20 like 1, transcript variant X9
PHD finger protein 20-like protein 1 isoform X10
PHD finger protein 20-like protein 1 isoform X9
PHD finger protein 20-like protein 1 isoform X6
PHD finger protein 20-like protein 1 isoform X5
PHD finger protein 20-like protein 1 isoform X4
PHD finger protein 20-like protein 1 isoform X2
PHD finger protein 20-like protein 1 isoform X8
PHD finger protein 20-like protein 1 isoform X3
PHD finger protein 20-like protein 1 isoform X1
PHD finger protein 20-like protein 1 isoform X7
PHD finger protein 20 like 1, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
PHD finger protein 20-like protein 1 isoform X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane protein 71, transcript variant X2
transmembrane protein 71, transcript variant X1
transmembrane protein 71, transcript variant X6
transmembrane protein 71, transcript variant X3
transmembrane protein 71, transcript variant X4
transmembrane protein 71, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium voltage-gated channel subfamily Q member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 Proteins
potassium voltage-gated channel subfamily KQT member 3
COORDINATES: nucleotide motif:Rfam:12.0:RF00561
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
adenylate cyclase 8, transcript variant X1
adenylate cyclase 8, transcript variant X2
adenylate cyclase 8, transcript variant X3
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X1
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X3
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X2
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X4
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X3
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X4
CYFIP related Rac1 interactor B, transcript variant X2
CYFIP related Rac1 interactor B, transcript variant X3
CYFIP related Rac1 interactor B, transcript variant X1
CYFIP-related Rac1 interactor B isoform X2
CYFIP-related Rac1 interactor B isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125360447, transcript variant X3
uncharacterized LOC125360447, transcript variant X1
uncharacterized LOC125360447, transcript variant X2
MYC proto-oncogene, bHLH transcription factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00438
uncharacterized LOC125360489, transcript variant X2
uncharacterized LOC125360489, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WASH complex subunit 5, transcript variant X1
WASH complex subunit 5, transcript variant X2
MTSS I-BAR domain containing 1, transcript variant X1
MTSS I-BAR domain containing 1, transcript variant X3
MTSS I-BAR domain containing 1, transcript variant X4
MTSS I-BAR domain containing 1, transcript variant X6
MTSS I-BAR domain containing 1, transcript variant X2
MTSS I-BAR domain containing 1, transcript variant X5
MTSS I-BAR domain containing 1, transcript variant X7
NADH:ubiquinone oxidoreductase subunit B9
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9
TatD DNase domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
TatD DNase domain containing 1, transcript variant X2
TatD DNase domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tRNA wybutosine-synthesizing protein 2 homolog
transmembrane protein 65, transcript variant X1
transmembrane protein 65, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: fer-1-like protein 6
family with sequence similarity 91 member A1, transcript variant X1
family with sequence similarity 91 member A1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 12 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
kelch like family member 38, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
kelch like family member 38, transcript variant X1
protein N-terminal glutamine amidohydrolase
ATPase family AAA domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ATPase family AAA domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATPase family AAA domain-containing protein 2 isoform X1
ATPase family AAA domain-containing protein 2 isoform X2
ATPase family AAA domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ATPase family AAA domain-containing protein 2 isoform X3
LOW QUALITY PROTEIN: zinc fingers and homeoboxes protein 1
chromosome 12 C8orf76 homolog, transcript variant X1
chromosome 12 C8orf76 homolog, transcript variant X2
uncharacterized protein C8orf76 homolog isoform X1
uncharacterized protein C8orf76 homolog isoform X2
family with sequence similarity 83 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TBC1 domain family member 31, transcript variant X1
TBC1 domain family member 31, transcript variant X3
TBC1 domain family member 31, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TBC1 domain family member 31, transcript variant X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00430
26S proteasome complex subunit SEM1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc fingers and homeoboxes 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc fingers and homeoboxes 2, transcript variant X1
zinc fingers and homeoboxes 2, transcript variant X4
zinc fingers and homeoboxes 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00432
solute carrier family 22 member 22-like, transcript variant X2
solute carrier family 22 member 22-like, transcript variant X1
solute carrier family 22 member 22-like isoform X2
solute carrier family 22 member 22-like isoform X1
solute carrier family 22 member 22-like, transcript variant X4
solute carrier family 22 member 22-like, transcript variant X3
solute carrier family 22 member 22-like isoform X4
solute carrier family 22 member 22-like isoform X3
26S proteasome non-ATPase regulatory subunit 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
hyaluronan synthase 2, transcript variant X1
hyaluronan synthase 2, transcript variant X2
coiled-coil-helix-coiled-coil-helix domain-containing protein 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L13, mitochondrial
collagen type XIV alpha 1 chain, transcript variant X4
collagen type XIV alpha 1 chain, transcript variant X1
collagen type XIV alpha 1 chain, transcript variant X3
collagen type XIV alpha 1 chain, transcript variant X2
collagen type XIV alpha 1 chain, transcript variant X5
DEP domain containing MTOR interacting protein
DEP domain-containing mTOR-interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
DNA replication and sister chromatid cohesion 1
ankyrin repeat and SOCS box protein 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
TATA-box binding protein associated factor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transcription initiation factor TFIID subunit 2
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X2
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X2
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X1
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X3
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X4
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X5
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X6
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X7
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X1
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X4
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X3
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X5
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X6
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 11B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
sterile alpha motif domain containing 12, transcript variant X5
sterile alpha motif domain containing 12, transcript variant X3
sterile alpha motif domain containing 12, transcript variant X4
sterile alpha motif domain containing 12, transcript variant X2
sterile alpha motif domain containing 12, transcript variant X1
sterile alpha motif domain containing 12, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sterile alpha motif domain containing 12, transcript variant X7
sterile alpha motif domain-containing protein 12 isoform X5
sterile alpha motif domain-containing protein 12 isoform X7
sterile alpha motif domain-containing protein 12 isoform X3
sterile alpha motif domain-containing protein 12 isoform X2
sterile alpha motif domain-containing protein 12 isoform X4
sterile alpha motif domain-containing protein 12 isoform X1
sterile alpha motif domain-containing protein 12 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
alanine and arginine rich domain containing protein
alanine and arginine-rich domain-containing protein
double-strand-break repair protein rad21 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
UTP23 small subunit processome component
eukaryotic translation initiation factor 3 subunit H
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
transcriptional repressor GATA binding 1, transcript variant X1
transcriptional repressor GATA binding 1, transcript variant X7
transcriptional repressor GATA binding 1, transcript variant X11
transcriptional repressor GATA binding 1, transcript variant X4
transcriptional repressor GATA binding 1, transcript variant X10
transcriptional repressor GATA binding 1, transcript variant X8
transcriptional repressor GATA binding 1, transcript variant X5
transcriptional repressor GATA binding 1, transcript variant X3
zinc finger transcription factor Trps1 isoform X3
transcriptional repressor GATA binding 1, transcript variant X9
transcriptional repressor GATA binding 1, transcript variant X2
transcriptional repressor GATA binding 1, transcript variant X6
zinc finger transcription factor Trps1 isoform X4
zinc finger transcription factor Trps1 isoform X1
zinc finger transcription factor Trps1 isoform X5
zinc finger transcription factor Trps1 isoform X8
zinc finger transcription factor Trps1 isoform X2
zinc finger transcription factor Trps1 isoform X7
zinc finger transcription factor Trps1 isoform X6
CUB and Sushi multiple domains 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
CUB and Sushi multiple domains 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
CUB and Sushi multiple domains 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 10% coverage of the annotated genomic feature by RNAseq alignments
CUB and sushi domain-containing protein 3 isoform X1
CUB and sushi domain-containing protein 3 isoform X2
CUB and sushi domain-containing protein 3 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel modifier subfamily V member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily V member 1
nonsense-mediated mRNA decay factor SMG5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
estrogen receptor binding site associated antigen 9, transcript variant X3
estrogen receptor binding site associated antigen 9, transcript variant X2
estrogen receptor binding site associated antigen 9, transcript variant X1
receptor-binding cancer antigen expressed on SiSo cells isoform X2
receptor-binding cancer antigen expressed on SiSo cells isoform X1
receptor-binding cancer antigen expressed on SiSo cells isoform X3
ENY2 transcription and export complex 2 subunit, transcript variant X2
ENY2 transcription and export complex 2 subunit, transcript variant X1
transcription and mRNA export factor ENY2 isoform X1
transcription and mRNA export factor ENY2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 3 subunit E
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
oxidation resistance 1, transcript variant X1
oxidation resistance 1, transcript variant X3
oxidation resistance 1, transcript variant X6
oxidation resistance 1, transcript variant X5
oxidation resistance 1, transcript variant X2
oxidation resistance 1, transcript variant X4
oxidation resistance 1, transcript variant X7
oxidation resistance 1, transcript variant X8
oxidation resistance 1, transcript variant X9
oxidation resistance protein 1 isoform X3
oxidation resistance protein 1 isoform X1
oxidation resistance protein 1 isoform X5
oxidation resistance protein 1 isoform X4
oxidation resistance protein 1 isoform X2
oxidation resistance protein 1 isoform X6
oxidation resistance protein 1 isoform X8
oxidation resistance protein 1 isoform X7
zinc finger protein, FOG family member 2, transcript variant X1
zinc finger protein, FOG family member 2, transcript variant X2
WD repeat and SOCS box-containing protein 1-like
LDL receptor related protein 12, transcript variant X1
LDL receptor related protein 12, transcript variant X2
low-density lipoprotein receptor-related protein 12 isoform X1
low-density lipoprotein receptor-related protein 12 isoform X2
dihydropyrimidinase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
dihydropyrimidinase, transcript variant X6
dihydropyrimidinase, transcript variant X5
dihydropyrimidinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dihydropyrimidinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
dihydropyrimidinase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
dendrocyte expressed seven transmembrane protein, transcript variant X3
dendrocyte expressed seven transmembrane protein, transcript variant X4
dendrocyte expressed seven transmembrane protein, transcript variant X2
dendrocyte expressed seven transmembrane protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
dendritic cell-specific transmembrane protein isoform X3
dendritic cell-specific transmembrane protein isoform X4
dendritic cell-specific transmembrane protein isoform X2
dendritic cell-specific transmembrane protein isoform X1
regulating synaptic membrane exocytosis 2, transcript variant X3
regulating synaptic membrane exocytosis 2, transcript variant X2
regulating synaptic membrane exocytosis 2, transcript variant X4
regulating synaptic membrane exocytosis 2, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X9
regulating synaptic membrane exocytosis 2, transcript variant X21
regulating synaptic membrane exocytosis 2, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X14
regulating synaptic membrane exocytosis 2, transcript variant X5
regulating synaptic membrane exocytosis 2, transcript variant X28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X36
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X33
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X31
regulating synaptic membrane exocytosis 2, transcript variant X23
regulating synaptic membrane exocytosis 2, transcript variant X34
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X35
regulating synaptic membrane exocytosis 2, transcript variant X32
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 5 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X37
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 2, transcript variant X39
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulating synaptic membrane exocytosis 2, transcript variant X38
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis protein 2 isoform X16
regulating synaptic membrane exocytosis protein 2 isoform X3
regulating synaptic membrane exocytosis protein 2 isoform X12
regulating synaptic membrane exocytosis protein 2 isoform X2
regulating synaptic membrane exocytosis protein 2 isoform X25
regulating synaptic membrane exocytosis protein 2 isoform X19
regulating synaptic membrane exocytosis protein 2 isoform X6
regulating synaptic membrane exocytosis protein 2 isoform X17
regulating synaptic membrane exocytosis protein 2 isoform X7
regulating synaptic membrane exocytosis protein 2 isoform X13
regulating synaptic membrane exocytosis protein 2 isoform X22
regulating synaptic membrane exocytosis protein 2 isoform X9
regulating synaptic membrane exocytosis protein 2 isoform X21
regulating synaptic membrane exocytosis protein 2 isoform X15
regulating synaptic membrane exocytosis protein 2 isoform X8
regulating synaptic membrane exocytosis protein 2 isoform X4
regulating synaptic membrane exocytosis protein 2 isoform X11
regulating synaptic membrane exocytosis protein 2 isoform X1
regulating synaptic membrane exocytosis protein 2 isoform X10
regulating synaptic membrane exocytosis protein 2 isoform X14
regulating synaptic membrane exocytosis protein 2 isoform X5
regulating synaptic membrane exocytosis protein 2 isoform X28
regulating synaptic membrane exocytosis protein 2 isoform X27
regulating synaptic membrane exocytosis protein 2 isoform X36
regulating synaptic membrane exocytosis protein 2 isoform X26
regulating synaptic membrane exocytosis protein 2 isoform X33
regulating synaptic membrane exocytosis protein 2 isoform X24
regulating synaptic membrane exocytosis protein 2 isoform X31
regulating synaptic membrane exocytosis protein 2 isoform X23
regulating synaptic membrane exocytosis protein 2 isoform X34
regulating synaptic membrane exocytosis protein 2 isoform X30
regulating synaptic membrane exocytosis protein 2 isoform X18
regulating synaptic membrane exocytosis protein 2 isoform X29
regulating synaptic membrane exocytosis protein 2 isoform X35
regulating synaptic membrane exocytosis protein 2 isoform X32
regulating synaptic membrane exocytosis protein 2 isoform X20
regulating synaptic membrane exocytosis protein 2 isoform X37
regulating synaptic membrane exocytosis protein 2 isoform X39
regulating synaptic membrane exocytosis protein 2 isoform X38
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
mitochondrial folate transporter/carrier
collagen triple helix repeat containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
collagen triple helix repeat containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
collagen triple helix repeat-containing protein 1 isoform X2
collagen triple helix repeat-containing protein 1 isoform X1
frizzled class receptor 6, transcript variant X2
frizzled class receptor 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
brain and acute leukemia cytoplasmic protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
antizyme inhibitor 1, transcript variant X1
antizyme inhibitor 1, transcript variant X3
antizyme inhibitor 1, transcript variant X2
antizyme inhibitor 1, transcript variant X4
outer dense fiber of sperm tails 1, transcript variant X2
outer dense fiber of sperm tails 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
ubiquitin protein ligase E3 component n-recognin 5, transcript variant X4
ubiquitin protein ligase E3 component n-recognin 5, transcript variant X1
ubiquitin protein ligase E3 component n-recognin 5, transcript variant X2
ubiquitin protein ligase E3 component n-recognin 5, transcript variant X3
E3 ubiquitin-protein ligase UBR5 isoform X1
E3 ubiquitin-protein ligase UBR5 isoform X2
E3 ubiquitin-protein ligase UBR5 isoform X3
E3 ubiquitin-protein ligase UBR5 isoform X4
ribonucleotide reductase regulatory TP53 inducible subunit M2B, transcript variant X1
ribonucleotide reductase regulatory TP53 inducible subunit M2B, transcript variant X2
ribonucleotide reductase regulatory TP53 inducible subunit M2B, transcript variant X6
ribonucleoside-diphosphate reductase subunit M2 B isoform X1
ribonucleoside-diphosphate reductase subunit M2 B isoform X3
ribonucleotide reductase regulatory TP53 inducible subunit M2B, transcript variant X4
ribonucleotide reductase regulatory TP53 inducible subunit M2B, transcript variant X3
ribonucleotide reductase regulatory TP53 inducible subunit M2B, transcript variant X5
ribonucleoside-diphosphate reductase subunit M2 B isoform X2
neurocalcin delta, transcript variant X2
neurocalcin delta, transcript variant X1
neurocalcin delta, transcript variant X3
grainyhead like transcription factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
grainyhead like transcription factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
grainyhead-like protein 2 homolog isoform X1
grainyhead-like protein 2 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 706, transcript variant X2
zinc finger protein 706, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125360430, transcript variant X1
uncharacterized LOC125360430, transcript variant X2
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ankyrin repeat domain 46, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ankyrin repeat domain 46, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ankyrin repeat domain 46, transcript variant X1
ankyrin repeat domain-containing protein 46
ring finger protein 19A, RBR E3 ubiquitin protein ligase, transcript variant X1
ring finger protein 19A, RBR E3 ubiquitin protein ligase, transcript variant X2
DNA-directed RNA polymerases I, II, and III subunit RPABC4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
vacuolar protein sorting 13 homolog B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
vacuolar protein sorting 13 homolog B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
vacuolar protein sorting 13 homolog B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
vacuolar protein sorting 13 homolog B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
vacuolar protein sorting 13 homolog B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
vacuolar protein sorting 13 homolog B, transcript variant X4
vacuolar protein sorting-associated protein 13B isoform X2
vacuolar protein sorting-associated protein 13B isoform X1
vacuolar protein sorting-associated protein 13B isoform X3
vacuolar protein sorting 13 homolog B, transcript variant X7
vacuolar protein sorting-associated protein 13B isoform X4
vacuolar protein sorting 13 homolog B, transcript variant X8
vacuolar protein sorting-associated protein 13B isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 216 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
odd-skipped related transciption factor 2, transcript variant X3
odd-skipped related transciption factor 2, transcript variant X1
odd-skipped related transciption factor 2, transcript variant X2
protein odd-skipped-related 2 isoform X1
protein odd-skipped-related 2 isoform X3
protein odd-skipped-related 2 isoform X2
potassium voltage-gated channel modifier subfamily S member 2
potassium voltage-gated channel subfamily S member 2
NIPA like domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NIPA like domain containing 2, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
POP1 homolog, ribonuclease P/MRP subunit
ribonucleases P/MRP protein subunit POP1
reactive intermediate imine deaminase A homolog
2-iminobutanoate/2-iminopropanoate deaminase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00139
lysosomal-associated transmembrane protein 4B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
testis-specific Y-encoded-like protein 5
carboxypeptidase Q, transcript variant X2
carboxypeptidase Q, transcript variant X1
carboxypeptidase Q, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
peptidyl-prolyl cis-trans isomerase A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial transcription termination factor 3, transcript variant X1
mitochondrial transcription termination factor 3, transcript variant X2
transcription termination factor 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
developmental pluripotency-associated 5 protein
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cilia and flagella associated protein 418, transcript variant X2
cilia and flagella associated protein 418, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
cilia- and flagella-associated protein 418 isoform X1
cilia- and flagella-associated protein 418 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase RING2-like
S-phase kinase-associated protein 1-like
CCR4-NOT transcription complex subunit 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology and FYVE domain containing 2, transcript variant X2
pleckstrin homology and FYVE domain containing 2, transcript variant X5
pleckstrin homology and FYVE domain containing 2, transcript variant X1
pleckstrin homology and FYVE domain containing 2, transcript variant X4
pleckstrin homology and FYVE domain containing 2, transcript variant X3
pleckstrin homology and FYVE domain containing 2, transcript variant X6
pleckstrin homology domain-containing family F member 2 isoform X1
pleckstrin homology and FYVE domain containing 2, transcript variant X7
pleckstrin homology domain-containing family F member 2 isoform X2
low molecular weight phosphotyrosine protein phosphatase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X1
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X2
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X4
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X3
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X1
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X2
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X3
tumor protein p53 inducible nuclear protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
tumor protein p53 inducible nuclear protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
tumor protein p53 inducible nuclear protein 1, transcript variant X1
tumor protein p53-inducible nuclear protein 1 isoform X1
tumor protein p53-inducible nuclear protein 1 isoform X2
integrator complex subunit 8, transcript variant X1
integrator complex subunit 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
epithelial splicing regulatory protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
epithelial splicing regulatory protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
epithelial splicing regulatory protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
epithelial splicing regulatory protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
epithelial splicing regulatory protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
epithelial splicing regulatory protein 1 isoform X3
epithelial splicing regulatory protein 1 isoform X5
epithelial splicing regulatory protein 1 isoform X4
epithelial splicing regulatory protein 1 isoform X2
epithelial splicing regulatory protein 1 isoform X1
vir like m6A methyltransferase associated, transcript variant X1
vir like m6A methyltransferase associated, transcript variant X3
vir like m6A methyltransferase associated, transcript variant X2
vir like m6A methyltransferase associated, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DNA repair and recombination protein RAD54B isoform X1
DNA repair and recombination protein RAD54B isoform X2
DNA repair and recombination protein RAD54B isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
GTP binding protein overexpressed in skeletal muscle, transcript variant X2
GTP binding protein overexpressed in skeletal muscle, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
pyruvate dehydrogenase phosphatase catalytic subunit 1, transcript variant X3
pyruvate dehydrogenase phosphatase catalytic subunit 1, transcript variant X2
pyruvate dehydrogenase phosphatase catalytic subunit 1, transcript variant X1
pyruvate dehyrogenase phosphatase catalytic subunit 1 isoform X1
pyruvate dehyrogenase phosphatase catalytic subunit 1 isoform X2
pyruvate dehyrogenase phosphatase catalytic subunit 1 isoform X3
transmembrane protein 67, transcript variant X2
transmembrane protein 67, transcript variant X1
transmembrane protein 67, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
CBY1 interacting BAR domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RNA binding motif protein 12B, transcript variant X5
RNA binding motif protein 12B, transcript variant X4
RNA binding motif protein 12B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RNA binding motif protein 12B, transcript variant X6
RNA binding motif protein 12B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RNA binding motif protein 12B, transcript variant X2
CBY1 interacting BAR domain containing 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CBY1 interacting BAR domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
CBY1 interacting BAR domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
CBY1 interacting BAR domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CBY1-interacting BAR domain-containing protein 1 isoform X2
CBY1-interacting BAR domain-containing protein 1 isoform X4
CBY1-interacting BAR domain-containing protein 1 isoform X3
CBY1-interacting BAR domain-containing protein 1 isoform X1
triple QxxK/R motif containing, transcript variant X1
triple QxxK/R motif containing, transcript variant X2
triple QxxK/R motif containing, transcript variant X3
triple QxxK/R motif containing, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
RUNX1 partner transcriptional co-repressor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 43 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RUNX1 partner transcriptional co-repressor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 31 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
RUNX1 partner transcriptional co-repressor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 43 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RUNX1 partner transcriptional co-repressor 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 31 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RUNX1 partner transcriptional co-repressor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 43 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RUNX1 partner transcriptional co-repressor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 31 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
leucine rich repeat containing 69, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeat containing 69, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 69 isoform X2
leucine-rich repeat-containing protein 69 isoform X1
phosphatidylinositol-4,5-bisphosphate 4-phosphatase 2, transcript variant X2
phosphatidylinositol-4,5-bisphosphate 4-phosphatase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
type 2 phosphatidylinositol 4,5-bisphosphate 4-phosphatase isoform X2
type 2 phosphatidylinositol 4,5-bisphosphate 4-phosphatase isoform X1
N-terminal EF-hand calcium binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
N-terminal EF-hand calcium-binding protein 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00554
2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing], mitochondrial
oxidative stress induced growth inhibitor family member 2, transcript variant X1
oxidative stress induced growth inhibitor family member 2, transcript variant X2
oxidative stress induced growth inhibitor family member 2, transcript variant X3
oxidative stress induced growth inhibitor family member 2, transcript variant X4
oxidative stress-induced growth inhibitor 2 isoform X1
oxidative stress-induced growth inhibitor 2 isoform X2
oxidative stress-induced growth inhibitor 2 isoform X3
receptor interacting serine/threonine kinase 2, transcript variant X2
receptor interacting serine/threonine kinase 2, transcript variant X1
receptor interacting serine/threonine kinase 2, transcript variant X3
receptor-interacting serine/threonine-protein kinase 2 isoform X2
receptor-interacting serine/threonine-protein kinase 2 isoform X1
receptor-interacting serine/threonine-protein kinase 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 15 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: vitamin D 25-hydroxylase-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
cyclic nucleotide binding domain containing 1
cyclic nucleotide-binding domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide gated channel subunit beta 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide-gated cation channel beta-3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
regulator of microtubule dynamics protein 1
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X5
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X1
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X4
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X2
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X3
NEDD4-like E3 ubiquitin-protein ligase WWP1 isoform X2
NEDD4-like E3 ubiquitin-protein ligase WWP1 isoform X1
LOW QUALITY PROTEIN: solute carrier family 7 member 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
ATPase H+ transporting V0 subunit d2, transcript variant X2
ATPase H+ transporting V0 subunit d2, transcript variant X1
V-type proton ATPase subunit d 2 isoform X2
V-type proton ATPase subunit d 2 isoform X1
protein serine kinase H2, transcript variant X2
protein serine kinase H2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
carbonic anhydrase 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
carbonic anhydrase 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
carbonic anhydrase 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ribosomal biogenesis factor, transcript variant X1
ribosomal biogenesis factor, transcript variant X2
E2F transcription factor 5, transcript variant X5
E2F transcription factor 5, transcript variant X3
E2F transcription factor 5, transcript variant X6
E2F transcription factor 5, transcript variant X4
E2F transcription factor 5, transcript variant X1
E2F transcription factor 5, transcript variant X2
E2F transcription factor 5, transcript variant X7
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X3
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X4
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X2
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X1
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X7
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X6
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X5
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X8
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X3
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X4
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X2
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X1
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X7
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X6
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X5
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein TRPC5OS homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger AN1-type containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
AN1-type zinc finger protein 1 isoform X1
zinc finger AN1-type containing 1, transcript variant X2
AN1-type zinc finger protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
fatty acid binding protein 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fatty acid binding protein 12, transcript variant X1
fatty acid-binding protein 12 isoform X2
fatty acid-binding protein 12 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
peripheral myelin protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
peripheral myelin protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 64% coverage of the annotated genomic feature by RNAseq alignments
vacuolar protein sorting-associated protein 4B-like
phosphoprotein membrane anchor with glycosphingolipid microdomains 1
phosphoprotein associated with glycosphingolipid-enriched microdomains 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 10
zinc finger and BTB domain-containing protein 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
tumor protein D52, transcript variant X2
tumor protein D52, transcript variant X1
28S ribosomal protein S28, mitochondrial
hes related family bHLH transcription factor with YRPW motif 1, transcript variant X1
hes related family bHLH transcription factor with YRPW motif 1, transcript variant X2
hairy/enhancer-of-split related with YRPW motif protein 1 isoform X1
hairy/enhancer-of-split related with YRPW motif protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycine cleavage system H protein, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
zinc finger C2HC-type containing 1A, transcript variant X1
zinc finger C2HC-type containing 1A, transcript variant X2
zinc finger C2HC domain-containing protein 1A isoform X2
zinc finger C2HC domain-containing protein 1A isoform X1
cAMP-dependent protein kinase inhibitor alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cAMP-dependent protein kinase inhibitor alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cAMP-dependent protein kinase inhibitor alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cAMP-dependent protein kinase inhibitor alpha isoform X1
cAMP-dependent protein kinase inhibitor alpha isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
cytochrome c oxidase assembly protein COX18, mitochondrial-like
uncharacterized LOC125360939, transcript variant X2
uncharacterized LOC125360939, transcript variant X1
peroxisomal biogenesis factor 2, transcript variant X3
peroxisomal biogenesis factor 2, transcript variant X1
peroxisomal biogenesis factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
zinc finger homeobox 4, transcript variant X2
zinc finger homeobox 4, transcript variant X3
zinc finger homeobox 4, transcript variant X1
zinc finger homeobox protein 4 isoform X2
zinc finger homeobox protein 4 isoform X1
hepatocyte nuclear factor 4 gamma, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
hepatocyte nuclear factor 4 gamma, transcript variant X3
hepatocyte nuclear factor 4 gamma, transcript variant X1
hepatocyte nuclear factor 4-gamma isoform X1
hepatocyte nuclear factor 4-gamma isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
cysteine rich secretory protein LCCL domain containing 1, transcript variant X1
cysteine rich secretory protein LCCL domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
cysteine-rich secretory protein LCCL domain-containing 1 isoform X1
cysteine-rich secretory protein LCCL domain-containing 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
ganglioside induced differentiation associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
ganglioside induced differentiation associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 18 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ganglioside-induced differentiation-associated protein 1 isoform X2
ganglioside-induced differentiation-associated protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lymphocyte antigen 96, transcript variant X2
lymphocyte antigen 96, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
staufen double-stranded RNA binding protein 2, transcript variant X7
staufen double-stranded RNA binding protein 2, transcript variant X6
staufen double-stranded RNA binding protein 2, transcript variant X3
staufen double-stranded RNA binding protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
staufen double-stranded RNA binding protein 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
double-stranded RNA-binding protein Staufen homolog 2 isoform X5
staufen double-stranded RNA binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
staufen double-stranded RNA binding protein 2, transcript variant X2
staufen double-stranded RNA binding protein 2, transcript variant X9
double-stranded RNA-binding protein Staufen homolog 2 isoform X2
staufen double-stranded RNA binding protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
double-stranded RNA-binding protein Staufen homolog 2 isoform X1
double-stranded RNA-binding protein Staufen homolog 2 isoform X4
double-stranded RNA-binding protein Staufen homolog 2 isoform X3
double-stranded RNA-binding protein Staufen homolog 2 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein L7, transcript variant X1
ribosomal protein L7, transcript variant X2
chromosome 12 C8orf89 homolog, transcript variant X1
chromosome 12 C8orf89 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
chromosome 12 C8orf89 homolog, transcript variant X3
putative uncharacterized protein C8orf89 homolog isoform X1
putative uncharacterized protein C8orf89 homolog isoform X2
putative uncharacterized protein C8orf89 homolog isoform X3
somatomedin B and thrombospondin type 1 domain containing
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
somatomedin-B and thrombospondin type-1 domain-containing protein
telomeric repeat binding factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
telomeric repeat binding factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
telomeric repeat-binding factor 1 isoform X2
telomeric repeat-binding factor 1 isoform X1
potassium voltage-gated channel subfamily B member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 13 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transient receptor potential cation channel subfamily A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
EYA transcriptional coactivator and phosphatase 1, transcript variant X5
EYA transcriptional coactivator and phosphatase 1, transcript variant X2
EYA transcriptional coactivator and phosphatase 1, transcript variant X3
EYA transcriptional coactivator and phosphatase 1, transcript variant X4
EYA transcriptional coactivator and phosphatase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
translocation associated membrane protein 1
translocating chain-associated membrane protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
proline-rich nuclear receptor coactivator 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: proline-rich nuclear receptor coactivator 2-like
protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1, transcript variant X1
protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1, transcript variant X2
protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1, transcript variant X3
protein-L-isoaspartate O-methyltransferase domain-containing protein 1 isoform X1
protein-L-isoaspartate O-methyltransferase domain-containing protein 1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01241
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ST18 C2H2C-type zinc finger transcription factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 47% coverage of the annotated genomic feature by RNAseq alignments
ST18 C2H2C-type zinc finger transcription factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
ST18 C2H2C-type zinc finger transcription factor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 44% coverage of the annotated genomic feature by RNAseq alignments
ST18 C2H2C-type zinc finger transcription factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
suppression of tumorigenicity 18 protein isoform X4
suppression of tumorigenicity 18 protein isoform X2
suppression of tumorigenicity 18 protein isoform X3
suppression of tumorigenicity 18 protein isoform X1
RB1 inducible coiled-coil 1, transcript variant X2
RB1 inducible coiled-coil 1, transcript variant X1
RB1-inducible coiled-coil protein 1 isoform X2
RB1-inducible coiled-coil protein 1 isoform X1
RB1 inducible coiled-coil 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00420
10 kDa heat shock protein, mitochondrial-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00108
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 35 Proteins
methionine--tRNA ligase, cytoplasmic-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
LOW QUALITY PROTEIN: methionine--tRNA ligase, cytoplasmic-like
ATPase H+ transporting V1 subunit H, transcript variant X2
ATPase H+ transporting V1 subunit H, transcript variant X1
ATPase H+ transporting V1 subunit H, transcript variant X3
V-type proton ATPase subunit H isoform X2
V-type proton ATPase subunit H isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: regulator of G-protein signaling 20
transcription elongation factor A1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transcription elongation factor A1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transcription elongation factor A protein 1 isoform X2
transcription elongation factor A protein 1 isoform X1
39S ribosomal protein L15, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 18% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00045
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 68, transcript variant X2
transmembrane protein 68, transcript variant X1
trimethylguanosine synthase 1, transcript variant X2
trimethylguanosine synthase 1, transcript variant X1
LYN proto-oncogene, Src family tyrosine kinase, transcript variant X2
LYN proto-oncogene, Src family tyrosine kinase, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF01277
PLAG1 zinc finger, transcript variant X4
PLAG1 zinc finger, transcript variant X1
PLAG1 zinc finger, transcript variant X2
PLAG1 zinc finger, transcript variant X3
coiled-coil-helix-coiled-coil-helix domain containing 7, transcript variant X1
coiled-coil-helix-coiled-coil-helix domain containing 7, transcript variant X2
coiled-coil-helix-coiled-coil-helix domain-containing protein 7
short chain dehydrogenase/reductase family 16C member 5
short-chain dehydrogenase/reductase family 16C member 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
3'(2'), 5'-bisphosphate nucleotidase 2, transcript variant X2
3'(2'), 5'-bisphosphate nucleotidase 2, transcript variant X1
Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 110 member B, transcript variant X2
family with sequence similarity 110 member B, transcript variant X1
UBX domain protein 2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
UBX domain protein 2B, transcript variant X2
UBX domain-containing protein 2B isoform X1
UBX domain-containing protein 2B isoform X2
UBX domain protein 2B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
UBX domain-containing protein 2B isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
neutral sphingomyelinase activation associated factor
thymocyte selection associated high mobility group box
thymocyte selection-associated high mobility group box protein TOX
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
RAB2A, member RAS oncogene family, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
RAB2A, member RAS oncogene family, transcript variant X1
chromodomain helicase DNA binding protein 7, transcript variant X1
chromodomain helicase DNA binding protein 7, transcript variant X5
chromodomain helicase DNA binding protein 7, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
chromodomain helicase DNA binding protein 7, transcript variant X3
chromodomain helicase DNA binding protein 7, transcript variant X2
chromodomain helicase DNA binding protein 7, transcript variant X4
chromodomain-helicase-DNA-binding protein 7 isoform X1
chromodomain-helicase-DNA-binding protein 7 isoform X2
chromodomain-helicase-DNA-binding protein 7 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 9% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 13 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
aspartate beta-hydroxylase, transcript variant X1
aspartyl/asparaginyl beta-hydroxylase isoform X1
aspartate beta-hydroxylase, transcript variant X2
aspartate beta-hydroxylase, transcript variant X3
aspartate beta-hydroxylase, transcript variant X5
aspartyl/asparaginyl beta-hydroxylase isoform X2
aspartyl/asparaginyl beta-hydroxylase isoform X5
aspartyl/asparaginyl beta-hydroxylase isoform X3
aspartate beta-hydroxylase, transcript variant X4
aspartyl/asparaginyl beta-hydroxylase isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium transporting ATPase interacting 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 15 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium-transporting ATPase subunit beta-1-interacting protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
YTH N6-methyladenosine RNA binding protein 3
LOW QUALITY PROTEIN: YTH domain-containing family protein 3
basic helix-loop-helix family member e22
class E basic helix-loop-helix protein 22
armadillo repeat containing 1, transcript variant X1
armadillo repeat containing 1, transcript variant X2
armadillo repeat-containing protein 1 isoform X1
armadillo repeat-containing protein 1 isoform X2
mitochondrial fission regulator 1, transcript variant X1
mitochondrial fission regulator 1, transcript variant X2
mitochondrial fission regulator 1 isoform X1
mitochondrial fission regulator 1, transcript variant X3
mitochondrial fission regulator 1 isoform X2
phosphodiesterase 7A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 9 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phosphodiesterase 7A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X1
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X2
uncharacterized LOC125360419, transcript variant X1
uncharacterized LOC125360419, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C5 beta
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ribosome biogenesis regulatory protein homolog
alcohol dehydrogenase iron containing 1, transcript variant X1
alcohol dehydrogenase iron containing 1, transcript variant X2
hydroxyacid-oxoacid transhydrogenase, mitochondrial isoform X1
hydroxyacid-oxoacid transhydrogenase, mitochondrial isoform X2
MYB proto-oncogene like 1, transcript variant X1
MYB proto-oncogene like 1, transcript variant X2
valosin containing protein interacting protein 1
serum/glucocorticoid regulated kinase family member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
serum/glucocorticoid regulated kinase family member 3, transcript variant X1
serine/threonine-protein kinase Sgk3 isoform X2
serine/threonine-protein kinase Sgk3 isoform X1
minichromosome maintenance domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
minichromosome maintenance domain-containing protein 2
protein phosphatase 1 regulatory subunit 42
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
centrosome and spindle pole associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
centrosome and spindle pole associated protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
centrosome and spindle pole associated protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
centrosome and spindle pole associated protein 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
centrosome and spindle pole associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
centrosome and spindle pole associated protein 1, transcript variant X6
centrosome and spindle pole associated protein 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
centrosome and spindle pole associated protein 1, transcript variant X5
centrosome and spindle pole associated protein 1, transcript variant X8
centrosome and spindle pole-associated protein 1 isoform X1
centrosome and spindle pole-associated protein 1 isoform X3
centrosome and spindle pole-associated protein 1 isoform X4
centrosome and spindle pole-associated protein 1 isoform X7
centrosome and spindle pole-associated protein 1 isoform X2
centrosome and spindle pole-associated protein 1 isoform X6
centrosome and spindle pole-associated protein 1 isoform X5
ADP ribosylation factor guanine nucleotide exchange factor 1
brefeldin A-inhibited guanine nucleotide-exchange protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2
phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
solute carrier organic anion transporter family member 5A1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor coactivator 2, transcript variant X3
nuclear receptor coactivator 2, transcript variant X2
nuclear receptor coactivator 2, transcript variant X1
nuclear receptor coactivator 2, transcript variant X5
nuclear receptor coactivator 2, transcript variant X4
nuclear receptor coactivator 2 isoform X5
nuclear receptor coactivator 2 isoform X4
nuclear receptor coactivator 2 isoform X3
nuclear receptor coactivator 2 isoform X2
nuclear receptor coactivator 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins